doCRMAv1 {aroma.affymetrix} | R Documentation |
Estimation and assessment of raw copy numbers at the single locus level (CRMA v1)
Description
Estimation and assessment of raw copy numbers at the single locus level (CRMA v1) based on [1]. The algorithm is processed in bounded memory, meaning virtually any number of arrays can be analyzed on also very limited computer systems.
Usage
## S3 method for class 'AffymetrixCelSet'
doCRMAv1(csR, shift=+300, combineAlleles=TRUE, lengthRange=NULL, arrays=NULL, drop=TRUE,
verbose=FALSE, ...)
## Default S3 method:
doCRMAv1(dataSet, ..., verbose=FALSE)
## Default S3 method:
doASCRMAv1(...)
Arguments
csR , dataSet |
An |
shift |
An tuning parameter specifying how much to shift the probe signals before probe summarization. |
combineAlleles |
A |
lengthRange |
An optional |
arrays |
A |
drop |
If |
verbose |
See |
... |
Additional arguments used to set up |
Value
Returns a named list
, iff drop == FALSE
, otherwise
only ChipEffectSet
object.
Allele-specific or only total-SNP signals
If you wish to obtain allele-specific estimates for SNPs, which
are needed to call genotypes or infer parent-specific copy numbers,
then use argument combineAlleles=FALSE
. Total copy number
signals are still available.
If you know for certain that you will not use allele-specific
estimates, you will get slightly less noisy signals
(very small difference) if you use combineAlleles=TRUE
.
doASCRMAv1(...)
is a wrapper for
doCRMAv1(..., combineAlleles=FALSE)
.
Author(s)
Henrik Bengtsson
References
[1] H. Bengtsson, R. Irizarry, B. Carvalho & T.P. Speed.
Estimation and assessment of raw copy numbers at the
single locus level,
Bioinformatics, 2008.
See Also
For CRMA v2 (recommended by authors), which is a single-array
improvement over CRMA v1, see doCRMAv2
().